Difference between revisions of "Nexalign"
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Revision as of 11:25, 9 June 2010
Application data |
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Principal bioinformatics method(s) | Mapping |
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Maintained? | Maybe |
Licence | GPL |
Operating system(s) | Unix |
Summary: Nexalign is a program to align millions of short reads from next-generation sequencing data sets to reference genomes
"Error: no local variable "counter" was set." is not a number.
Links
References
none specified
To add a reference for Nexalign, enter the PubMed ID in the field below and click 'Add'.